Align alginate biosynthesis protein AlgA; EC 2.7.7.13; EC 5.3.1.8 (characterized)
to candidate WP_152527971.1 N177_RS18150 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= CharProtDB::CH_121570 (483 letters) >NCBI__GCF_000496075.1:WP_152527971.1 Length = 462 Score = 409 bits (1051), Expect = e-118 Identities = 219/465 (47%), Positives = 293/465 (63%), Gaps = 6/465 (1%) Query: 6 LSGGSGSRLWPLSRKQFPKQFLALTGE-HTLFQQTLERLVFEGMDTPIVVCNKDHRFIVN 64 ++GG+G+RLWPLSR PKQF+AL E + FQ TL R+ G D PIVV N D RFI Sbjct: 1 MAGGAGTRLWPLSRDTMPKQFIALLDEGQSTFQATLRRVAARGFDRPIVVTNHDFRFICA 60 Query: 65 EQLANRKLECQRILMEPFGRNTAPAVALTAMMLVNEGRDELMLVLPADHVIDDQKALQRA 124 EQ+ +E I++EP R++A AVA+ A++ D + VL +DHV+ ++ L A Sbjct: 61 EQMQGIGIEGD-IVLEPERRDSAAAVAVGALLAHRRNPDSVCAVLASDHVVTQEEGLLDA 119 Query: 125 LALATVAAERGEMVLFGVPATRPETGYGYIKSTNDSLLPEGVSR-VQQFVEKPDEKRAVE 183 + A AA G ++ G+ + YGYI+ +++ G +R + +FVEKPD + A Sbjct: 120 IREAAAAARGGWIMTLGITPDHASSAYGYIQPAEEAI--SGRARAITRFVEKPDVETAQR 177 Query: 184 FVKSGGYFWNSGMFLFRASRFLEELKKHDPDIYDTCVLTLERSEQTADTVTLDDATFACC 243 ++ G Y WNSG F+F A L+EL H P++ + LE + + D + LD A+FA C Sbjct: 178 YLDEG-YSWNSGNFVFGAELMLQELHAHAPEVLEGARDALEGATRDLDFLRLDQASFARC 236 Query: 244 PDNSIDYAVMEKTQRACVVPLSAGWSDVGCWASLWAVNDKDIHGNVSKGDVVIQDSRNCM 303 P SIDYAVMEKTQ V+ GWSD+G W SL A+ KD GNV +GDV D+ N Sbjct: 237 PRISIDYAVMEKTQAGGVLAAEFGWSDIGSWDSLHAMKAKDTSGNVLEGDVRAIDTTNSF 296 Query: 304 IHGNGKLVSVIGLDNIVVVETKDAMMIAHKDKVQGVKQMVSTLNDQGRSETQNHCEVYRP 363 + + L +V+GLD+ VVV T DA+++A + V VK++V+ L +GR E H V+RP Sbjct: 297 VRSDNMLTTVLGLDSAVVVTTHDAVLVAARSHVAEVKRLVAQLAGEGRREAGEHLRVHRP 356 Query: 364 WGSYDSVDMGGRFQVKHISVKPGACLSLQMHHHRAEHWIVVSGTAEVTCDENVFLLTENQ 423 WG Y +D+G FQVKHI VKPG LSLQ H HRAEHW+VV GTAEVT D V L EN+ Sbjct: 357 WGWYQRIDIGAGFQVKHICVKPGGVLSLQRHFHRAEHWVVVRGTAEVTLDGKVALYHENE 416 Query: 424 STYIPIASVHRLRNPGKIPLEIIEVQSGSYLGEDDIERFEDIYGR 468 + YIP+ +VHRL NPGKI L++IEVQ GSY GEDDI R ED+Y R Sbjct: 417 AAYIPVGAVHRLHNPGKIDLKLIEVQVGSYTGEDDIVRIEDVYSR 461 Lambda K H 0.319 0.135 0.405 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 544 Number of extensions: 22 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 483 Length of database: 462 Length adjustment: 33 Effective length of query: 450 Effective length of database: 429 Effective search space: 193050 Effective search space used: 193050 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory